| Product NDC: | 52584-025 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | Sodium Chloride |
| Active Ingredient(s): | 234 mg/30mL & nbsp; Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52584-025 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111026 |
| Package NDC: | 52584-025-30 |
| Package Description: | 1 VIAL in 1 BAG (52584-025-30) > 30 mL in 1 VIAL |
| NDC Code | 52584-025-30 |
| Proprietary Name | Sodium Chloride |
| Package Description | 1 VIAL in 1 BAG (52584-025-30) > 30 mL in 1 VIAL |
| Product NDC | 52584-025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111026 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 234 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |